Retinal isoforms of inosine 5'-monophosphate dehydrogenase type 1 are poor nucleic acid binding proteins (Q24647325)

1

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Garrett Cobb

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Catherine J Spellicy

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Sara J Bowne

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Lizbeth Hedstrom

Archives of Biochemistry and Biophysics

6

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language of work or name

English

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publication date

15 April 2008

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published in

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volume

472

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issue

2

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page(s)

100-4

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cites work

Why do mutations in the ubiquitously expressed housekeeping gene IMPDH1 cause retina-specific photoreceptor degeneration?

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Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis

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Autosomal dominant retinitis pigmentosa mutations in inosine 5'-monophosphate dehydrogenase type I disrupt nucleic acid binding

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Inosine 5'-monophosphate dehydrogenase binds nucleic acids in vitro and in vivo

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Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa

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Crystal structure of a ternary complex of Tritrichomonas foetus inosine 5'-monophosphate dehydrogenase: NAD+ orients the active site loop for catalysis

7 April 2017

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Characterization of retinal inosine monophosphate dehydrogenase 1 in several mammalian species

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Screen of the IMPDH1 gene among patients with dominant retinitis pigmentosa and clinical features associated with the most common mutation, Asp226Asn

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Identification of an IMPDH1 mutation in autosomal dominant retinitis pigmentosa (RP10) revealed following comparative microarray analysis of transcripts derived from retinas of wild-type and Rho(-/-) mice

27 September 2017

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Biochemical analysis of the modular enzyme inosine 5'-monophosphate dehydrogenase

27 September 2017

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Selective up-regulation of type II inosine 5'-monophosphate dehydrogenase messenger RNA expression in human leukemias

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